A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3351186



Internal ID19782164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39131467..39133875hg38UCSC Ensembl
chr17:37287720..37290128hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382409
hg192409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14573956
SamplesHG02059
Known GenesPLXDC1
MethodSequencing
AnalysisRead and contig alignments were done with BLASR. The Celera assembler (8.3rc2) was used to assemble RS II samples (CHM1, CHM13, HG00514, HG00733, NA19240, HG02818, NA19434, HG01352, HG02059, NA12878, and HG04217, and Canu (1.7) was used for Sequel samples (HG02106 and HG00268). Variant calling was performed with SMRT-SV (10.1101/gr.214007.116).
PlatformPacBio RS II P6C4, PacBio Sequel v2.1
Comments
ReferenceAudano_et_al_2019
Pubmed ID30661756
Accession Number(s)nsv3351186
Frequency
Sample Size14
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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